نتایج جستجو برای: sickle cell anaemia
تعداد نتایج: 1695368 فیلتر نتایج به سال:
Abstract Background Prevalence of hereditary blood diseases such as sickle cell anemia, sickle thalassemia and thalassemia major are high in Khuzestan province. Sickle cell anemia and beta-thalassemia are predominantly common in Iranian Arabs. Pulmonary complications account for a large proportion of morbidity and mortality in patients with and sickle cell disease. Periodic lung function asse...
Low steady state haemoglobin oxygen saturation in patients with sickle cell anaemia has been associated with the degree of anaemia and haemolysis. How much pulmonary dysfunction contributes to low saturation is not clear. In a prospective study of children and adolescents with sickle cell disease aged 3-20 years at steady state and matched controls, 52% of 391 patients versus 24% of 63 controls...
I (ummins D, Heuischkcl R, Davies S. P'enicillin prophylaxis in children with sickle cell disease in 13rent. BAIJ 1991;302: 989-9(0. (27 April.) 2 Ferguson AD, Scott RB. Studies in sicklc cell anaemia. XIII. The management olt pneumonia in childrenl with sickle cell anemia. ,Medical Annals of the District of Columbil 1958;27:636-4 1. 3 Warlcy MA, Hamilton P'JS, Marsden PI), Brown RE, Miersellis...
Objective: To assess growth arrest-specific 6 (Gas6) protein as a biomarker of glomerular damage (glomerulopathy; nephropathy) in patients with sickle cell anaemia (SCA). Methods: seventy SCA on routine clinic visit and apparently healthy controls were recruited into the study their blood urine samples collected while plasma Gas6 well urinary albumin creatinine measured. Their socio-demographic...
Besides sickle-cell anaemia, the finding of Hb S with other /3-chain variants of adult haemoglobin was first demonstrated by Itano and Neel (1950) in the well-known discovery of sicklecell Hb C disease. Since then Hb S has been observed with Hb D, E, G, J. and K (Itano, 1951; Aksoy and Lehmann, 1957; Schwartz and Spaet, 1955 ; Went and MacIver, 1959; O'Gorman et al., 1963). In such circumstance...
A non-directive programme of prenatal counselling was used during a four year period. Forty-three couples at risk for having a baby with a haemoglobinopathy were identified. Prenatal diagnosis was offered in 19 pregnancies to 14 couples at risk of having a baby with sickle cell anaemia and in two pregnancies in two couples at risk of a baby with beta thalassaemia major, who presented before the...
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